K-number	K230239
Device name	AirSeal iFS System; AirSeal dV Solution
Applicant	Conmed Corporation
Product code	HIF
Device class	Class II
Decision date	Sep 20, 2023
Decision	Substantially Equivalent
Regulation	884.1730

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Source

View the full FDA submission: accessdata.fda.gov

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AirSeal iFS System; AirSeal dV Solution

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